VIGAMOX
- Product NDC
- 82667-700
- 11-digit product format
- 826670700
- Labeler code
- 82667
- Product ID
- 82667-700_48fbfef1-1e3b-4558-e063-6394a90a2454
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- moxifloxacin hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Harrow Eye, LLC
- Application
- NDA021598
- Marketing category
- NDA
- Marketing start
- 2024-07-01
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- VIGAMOX
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MOXIFLOXACIN HYDROCHLORIDE | 5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C53598599T |
| Rxcui | 403818, 404473 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82667-700-03 | VIGAMOX | 3 mL in 1 BOTTLE | SOLUTION/ DROPS | 3 | | 4 |
| 82667-700-03 | VIGAMOX | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82667-700 | VIGAMOX (MOXIFLOXACIN HYDROCHLORIDE) SOLUTION/ DROPS [HARROW EYE, LLC] | 1 | Current NDC, 2 package rows | 20240701_12053b08-7e66-c6f3-e063-6394a90a9cd9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82667-700-03 | 82667070003 | 1 BOTTLE in 1 CARTON (82667-700-03) / 3 mL in 1 BOTTLE | 1 bottle | 2024-07-01 | No | No | Historical |